- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03321162
Accuracy of Guided Implant Placement Using Double Versus Triple Scan Protocol in Completely Edentulous Patients
Accuracy of Guided Implant Placement Using Double Versus Triple Scan Protocol in Completely Edentulous Patients : Randomized Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In this study we discuss linear and angular deviation of actual implant position using planning protocol C1(double scan technique) or C2 (triple scan technique) in completely edentulous patient .
Both protocols C1(double scan technique) and C2 (triple scan technique) indicated in completely edentulous patient and require C.T scan for patient wearing scan appliance .
In C1(double scan technique) , after CT scan for patient wearing scan appliance , two optical scan for the model with and without scan appliance.
In C2 (triple scan technique) , after CT scan for patient wearing scan appliance , CT scan for scan appliance alone .
Teeth positions in both protocols were identified by radio-opaque scan appliance .
16 implant placement by surgical guide using double scan protocol versus triple scan protocol ( two groups - 8 implants in each group ) to Evaluate angular and linear deviation of virtual implants and actual implant position in completely edentulous patients according to scanning protocol C1(double scan technique) and C2 (triple scan technique) .
Study Type
Enrollment (Anticipated)
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients totally edentulous arches.
- patients with Bucco-lingual bone thickness >6 mm allowing flapless implant placement
- patients free from any systemic diseases that may affect bone quality e.g diabetes.
Exclusion Criteria:
- patients with thin ridges.
- patients with systemic disease that may affect bone quality.
- Patients with poor oral hygiene and active periodontal diseases.
- Anatomical situations requiring regenerative procedure.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
double scan protocol
In C1(double scan technique) , after CT scan for patient wearing scan appliance , two optical scan for the model with and without scan appliance.
|
|
|
triple scan protocol
In C2 (triple scan technique) , after CT scan for patient wearing scan appliance , CT scan for scan appliance alone .
|
Scanning strategy is based on multiple scans.
Essentially one CT scan of the patient (usually with a scan appliance).
Another CT scan of the model or scan appliance may be required (double scan technique).
Such a second CT scan can be replaced by optical scanning of the model and scan appliance (triple scan technique).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of angular deviation between planned implants in surgical guide and actual implant position in completely edentulous patients .
Time Frame: immediate post operative
|
Evaluation of angular deviation between planned implants in surgical guide and actual implant position in completely edentulous patients according to scanning protocol C1(double scan technique) and C2 (triple scan technique) .
|
immediate post operative
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of linear deviation between planned implants in surgical guide and actual implant position in completely edentulous patients
Time Frame: immediate post operative
|
Evaluation of linear deviation between planned implants in surgical guide and actual implant position in completely edentulous patients according to scanning protocol C1(double scan technique) and C2 (triple scan technique) .
|
immediate post operative
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Cebc.cu. cairo university
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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